FDA device listing
DYNA FEMALE GUARD INCONTINENCE PAD,DYNA HEAVY FLOW MATERNITY PAD WITH FIXATOR,DYNA MALE GUARD INCONTINENCE PAD,DYNA…
FDA device listing 1326560708 · DYNAMIC TECHNO MEDICALS PRIVATE LIMITED
Key facts
| Proprietary names | DYNA FEMALE GUARD INCONTINENCE PAD,DYNA HEAVY FLOW MATERNITY PAD WITH FIXATOR,DYNA MALE GUARD INCONTINENCE PAD,DYNA SANITARY PADS,DYNA SANITARY PADS WITH FIXATOR,NEWMOM DISPOSABLE MATERNITY MAXIPAD,NEWMOM DISPOSABLE MATERNITY MAXI PAD WITH FIXATOR,NEWMOM DISPOSABLE MATERNITY MEDIPAD,NEWMOM DISPOSABLE PAD FIXATOR,NEWMOM FIRST DAY MATERNITY SANITARY PAD WITH TIE ON,NEWMOM H DISPOSABLE MATERNITY MAXI… |
|---|---|
| Owner/operator | DYNAMIC TECHNO MEDICALS PRIVATE LIMITED |
| Owner/operator number | 10039773 |
| Product codes | HHD |
| Device names | HHD - Pad, Menstrual, Unscented |
| Device class | Class I |
| Classification regulations (21 CFR) | 884.5435 |
| Review panels | Obstetrics/Gynecology |
| Registered establishments | DYNAMIC TECHNO MEDICALS PRIVATE LIMITED |
| Establishment registrations | 3006227741 |
| FEI numbers | 3006227741 |
| Establishment operations | Contract Manufacturer, Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- None listed Premarket submission listed
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device listings
Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database